Výsledky vyhledávání - "Noemi Garrigos"

Co‐occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

Autor: Tatiana Molina, Ana Beatriz Sánchez-Heras, Virginia Díez-Obrero, Ángel Segura, Alan Codoñer-Alejos, Noemi Garrigos, José Luis Soto, Adela Castillejo, María Isabel Castillejo, Estela Dámaso, Rosario Ferrer-Avargues

Publikováno v: RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Cancer Communications
Cancer Communications, Vol 41, Iss 3, Pp 218-228 (2021)

Background Lynch syndrome (LS) is a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia associated with germline alterations in DNA mismatch repair genes. The classical genetic diagnostic st

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f88475c039757ff3236f57670b61bf2
http://hdl.handle.net/10045/114686

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Circulating tumour cell analysis as an early marker for relapse in stage II and III colorectal cancer patients: a pilot study

Autor: Miriam García-Bautista, Alfredo Carrato, Noemi Garrigos, Javier Gallego, José Luis Soto, Álvaro Rodríguez-Lescure, Ángeles Gómez-Martínez, Carmen Guillén-Ponce, Adela Castillejo, Patricia Guaraz

Publikováno v: CLINICAL & TRANSLATIONAL ONCOLOGY
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
instname
r-FISABIO. Repositorio Institucional de Producción Científica

Introduction Recent studies have identified both the prognostic and predictive utility of determining the number of circulating tumour cells (CTC) in patients with solid cancers. Material and methods In the present pilot study we evaluated the abilit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::923c5602d2c690cffb1dfdc888f60551
https://doi.org/10.1007/s12094-010-0479-7

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Akademický článek

Co‐occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

Autor: Rosario Ferrer‐Avargues, María Isabel Castillejo, Estela Dámaso, Virginia Díez‐Obrero, Noemí Garrigos, Tatiana Molina, Alan Codoñer‐Alejos, Ángel Segura, Ana Beatriz Sánchez‐Heras, Adela Castillejo, José Luis Soto

Publikováno v: Cancer Communications, Vol 41, Iss 3, Pp 218-228 (2021)

Abstract Background Lynch syndrome (LS) is a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia associated with germline alterations in DNA mismatch repair genes. The classical genetic diag

Externí odkaz: https://doaj.org/article/1ecd637319c94345af1605f294d9face

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